Acute Myeloid LeukemiaPhase 1BISECTNCT05456269
A Study of Bisantrene Combined With Cytarabine or With Decitabine for Adult Subjects With Extramedullary AML and MDS
A Phase 1 study testing Bisantrene Dihydrochloride (high dose), Bisantrene Dihydrochloride (low dose) and Cytarabine Hydrochloride in people with Acute Myeloid Leukemia and Recurrent Acute Myeloid Leukemia, run by Racura Oncology Ltd at 1 site in Australia.
Trial summary
This is a two strata Phase 1b study to assess the safety and efficacy of bisantrene (RC110) in combination with a) cytarabine arabinoside (Ara-C) treatment for patients with relapsed or refractory (R/R) Acute Myeloid Leukemia (AML) with extramedullary disease and able to tolerate intensive chemotherapy; b) in… Read more about this study
- Who is it for?
- Ages 18 years and older
- Conditions the study is for
- Acute Myeloid Leukemia, Recurrent Acute Myeloid Leukemia, Refractory Acute Myeloid Leukemia
- What is being tested?
- Bisantrene Dihydrochloride (high dose), Bisantrene Dihydrochloride (low dose) and Cytarabine Hydrochloride
- Type of treatment
- Pill or oral medicine, Injection or infusion
- Could I receive a placebo?
- No, everyone receives an active treatment
- How many people
- 0 participants
- Where
- 1 siteAustralia
- Study dates
- 29 Jul 2022to 31 Aug 2023
- Phase
- Phase 1
Key requirements
Who can take part, as listed by the sponsor. Only the study team can confirm whether you are eligible, so take this list to your doctor.
- Ages 18 years and older
- All sexes
- No healthy volunteers
- Adult, Older adult
Who may be able to join
- [Both Stratums]
- Patients must be able to understand and provide informed written consent.
- Patients must be of age ≥ 18 years at the time of signing the informed consent.
- Extramedullary disease (i.e., AML) by 18F-FDG PET/CT and/or clinical morphology (histopathology of chloroma, leukemia cutis or AML) at pre-screening
- Patients who have undergone stem cell transplantation (SCT), maybe included if they are ≥ 8 weeks from stem cell infusion (autologous or allogeneic), have no active graft versus host disease (GVHD), are off immune suppression for at least 2 weeks, and do not have a history of veno occlusive disease (VOD).
- Eastern Cooperative Oncology Group (ECOG) performance status ≤ 2.0 for intensive Stratum 1 patients and ≤ 3.0 for low intensity treatment Stratum 2 patients.
Show all 15Show fewer
- Life expectancy estimated to be > 3 months.
- Adequate organ function as evidenced by serum total bilirubin ≤ 2.0 mg/dL, alanine aminotransferase (ALT) or aspartate aminotransferase (AST) ≤ 5 × the upper limit of normal (ULN), serum creatinine ≤ 1.5 mg/dL or calculated creatinine clearance of ≥ 60 mL/min.
- Cardiac ejection fraction ≥ 50%, assessed by 2-Dimensional (2D) echocardiogram.
- Females of childbearing potential must have a negative serum pregnancy test at enrolment or within 14 days before study entry and must agree to use an adequate method of contraception, i.e., barrier method, during the study until 30 days after the last treatment. Males must be surgically or biologically sterile or agree to use an adequate method of contraception, i.e., barrier method, during the study until 30 days after the last treatment.
- [Stratum 1 only]
- Diagnosis of R/R AML, defined as ≥ 5% blasts in a patient with known prior history of AML according to World Health Organization (WHO) criteria. Patients with AML that have relapsed at least once or are primary induction failure will be eligible.
- [Stratum 2 only]
- Patients with diagnosis of de novo AML with EMD, or R/R AML with EMD.
- Patients with MDS or CMML, diagnosed according to the 2016 WHO classification with high-risk disease per the International Prognostic Scoring System (IPSS) of intermediate 2 or higher for both MDS and CMML. Revised IPSS intermediate risk patients can be considered after discussion with the Investigator.
Who cannot join
- [Both Stratums]
- Acute promyelocytic leukemia (APML) M3 subtype of AML.
- Central nervous system manifestations of AML, unless treated and with no residual manifestations (either by cerebrospinal fluid (CSF) cytology, radiologically or by other clinical assessments) in the last 2 weeks.
- Evidence or recent history of CNS disease, including primary or metastatic brain tumors, seizure disorders unless there is evidence for clearance of CNS leukemia (2 leukemia free CSFs by morphology and /or flow cytometry 1 week apart).
- Uncontrolled intercurrent illness including, but not limited to, ongoing or active infection, cirrhosis, chronic obstructive or restrictive pulmonary disease, symptomatic congestive heart failure, unstable angina pectoris, or cardiac arrhythmia.
- Other active malignancy (including other hematologic malignancies) or other malignancy within the last 12 months except non-melanoma skin cancer or cervical intraepithelial neoplasia.
- Major surgery within 4 weeks of treatment.
- Any medical, psychological, or social condition that may interfere with study patient or compliance or may compromise the patient's safety in the opinion of the Investigator.
Trial locations and contacts
1 site in 1 country.
About this study
Official title: An Open-label Two Strata Study of Bisantrene in Combination With Cytarabine Arabinoside or Bisantrene in Combination With Oral Decitabine/Cedazuridine for the Treatment of Acute Myeloid Leukemia Patients With Extramedullary Disease
This is a two strata Phase 1b study to assess the safety and efficacy of bisantrene (RC110) in combination with a) cytarabine arabinoside (Ara-C) treatment for patients with relapsed or refractory (R/R) Acute Myeloid Leukemia (AML) with extramedullary disease and able to tolerate intensive chemotherapy; b) in combination with decitabine/cedazuridune (ASTX727) new or relapsed or refractory AML or high risk MDS or CMML with extramedullary disease and unable or not willing to have intensive chemotherapy.
Read the detailed description
The study is a multicenter, open label in patients with haematological malignancy / myeloproliferative disease (AML, MDS and CMML) and extramedullary disease (EMD) investigating 2 treatment regimens:
- Stratum 1 will investigate use of high dose intravenous (IV) bisantrene (RC110) in combination with IV Ara-C for R/R AML with EMD able to tolerate intensive chemotherapy. This includes a run-in stage to confirm the dose of bisantrene (RC110) for induction and in combination with Ara-C for consolidation cycles and an expansion and an expansion stage that will treat additional patients at the confirmed bisantrene dose for induction and in combination with Ara-C consolidation cycles;
- Stratum 2 will investigate use lower doses intravenous (IV) bisantrene (RC-110) in combination with fixed-dose oral decitabine/cedazuridine (ASTX727) to determine the maximum tolerated dose (MTD) for new or R/R AML and HR-MDS/CMML unable to tolerate intensive chemotherapy.
Pre-screening will be conducted to identify patients with EMD diagnosed by standard clinical practice including histology and by fluorine-18-fluorodeoxyglucose positron emission tomography/computed tomography (18F FDG-PET/CT) imaging.
- Conditions
- Acute Myeloid Leukemia, Recurrent Acute Myeloid Leukemia, Refractory Acute Myeloid Leukemia, Higher Risk Myelodysplastic Syndrome, Chronic Myelomonocytic Leukemia
- Being tested
- Bisantrene Dihydrochloride (high dose), Bisantrene Dihydrochloride (low dose), Cytarabine Hydrochloride, Decitabine and cedazuridine
- Keywords
- combination treatment intervention
- Medical subject headings
- Leukemia, Myeloid, Acute, Leukemia, Myelomonocytic, Chronic
What participants receive
What participants receive. In a randomised study each person is assigned to one group by chance.
Bisantrene Dihydrochloride (high dose)Drug
Also called RC110, Zantrene®, Xantrene®
Induction monotherapy cycle: IV bisantrene daily on Days 1 to 7, starting at 250 mg/m2 then adjusted to either 275 mg/m2 or 225 mg/m2 based on confirmed dose (Run-in) Consolidation combination cycle/s: IV bisantrene daily on Days 1 to 2
Bisantrene Dihydrochloride (low dose)Drug
Also called RC110, Zantrene®, Xantrene®
IV bisantrene at escalating doses for 3 dose levels of 50, 65, 85 mg/m2 on Days 3 and 5 until Maximum tolerated dose (MTD) reached.
Cytarabine HydrochlorideDrug
Also called Ara-C, Cytarabine arabinoside, Cytosar-U®
Consolidation cycles: continuous IV cytarabine (100mg/m2) on Days 1 to 5
Decitabine and cedazuridineDrug
Also called ASTX727
PO fixed-dose decitabine/cedazuridine 35/100 mg tablet daily for 5 days (Days 1 to 5), 1 hour prior bisantrene infusion
| Study group | Role | What they receive |
|---|---|---|
| Stratum 1 | Experimental | Bisantrene infused daily for 7 days of induction cycle 1; followed by bisantrene infusion on Days 1 and 2 and cytarabine arabinoside continuous infusion on Days 1 to 5 of each consolidation cycle for up to 3 cycles.
Each cycle is 28 days, with a potential to expand to 42 days to allow for full hematologic recovery. Receives: Drug: Bisantrene Dihydrochloride (high dose); Drug: Cytarabine Hydrochloride |
| Stratum 2 | Experimental | Decitabine/cedazuridine daily on Days 1-5, Bisantrene infusion on Days 3 and 5 in 28 day cycle. Treatment repeats every 28 days up to 12 cycles in the absence of disease progression or unacceptable toxicity.
Each has potential to expand to 42 days to allow for full hematologic recovery. Receives: Drug: Bisantrene Dihydrochloride (low dose); Drug: Decitabine and cedazuridine |
What is being measured
The primary outcome is the main question the study is designed to answer.
Stratum 1, Stage 1: Dose confirmation
Maximum tolerated dose (MTD) based on occurence dose limiting toxicity (DLT) graded according to the National Cancer Institute Common Terminology Criteria (NCI CTCAE) for Adverse Events v5.0 after completion of 2 cycles of treatment
Measured: 8 weeks
Stratum 1 Stage 2: Overall response
Morphological overall response, defined as complete remission (CR), CR with incomplete hematologic recovery or morphologic leukemia free state (MLFS), after completion of first treatment cycle 1
Measured: 4 weeks
Stratum 2: Safety and tolerabillity
Assessed based on the occurence of non-hematological Dose limiting toxicity (DLT) as graded according to the National Cancer Institute Common Terminology Criteria (NCI CTCAE) for Adverse Events v5.0 at the completion of cycle 1.
Measured: 4 weeks
Secondary outcomes (15)
Stratum 1: Minimal Residual Disease (MRD) response
Response is defined as MRD negativity with and without morphological complete remission (CR), at low level molcular MRD with CR and MRD relapse (coversion MRD negativity to positivity) at the completion of cycle 1
Measured: 4 weeks
Stratum 1: Radiologic response
Response evaluation by 18F-FDG-PET/CT is based on the 5-point scale Deauville criteria for complete metabolic response (defined as Deauville Score (DS) 1, 2, or 3) or for partial metabolic response (defined DS of 4 or 5 with decrease in number or activity in bone marrow/EMD disease at the completion of cycles 1,2 and 4..
Measured: 4, 8 and 16 weeks
Stratum 1: Dermal clinical response
Dermal response based on improvement on the static investigator global assessment (IGA) 5-point disease severity scores, where higher score indicate more disease, defined as decrease of at least two points relative to baseline at the completion of cycles 1,2 3 and 4.
Measured: 4, 8, 12, and 16 weeks
Stratum 1: Dermal therapeutic response
Dermal therapeutic improvement based on the static investigator global assessment (IGA) 5-point disease severity scores, where higher score indicate more disease, defined as decrease of at least two points relative to baseline at the completion of cycles 1,2 3 and 4.
Measured: 4, 8, 12, and 16 weeks
Stratum 1: Safety and tolerability
Safety and tolerability based on the incidence and severity of adverse events assessed using National Cancer Institute-Common Terminology Criteria for Adverse Events [NCI-CTCAE] v5.0, grade per event, patient, and cycle of treatment.
Measured: 4, 8, 12 and 16 weeks
Stratum 1: Number of participants that recieve subsequent allogeneic hematopoietic stem cell transplant
Proportion of patients who receive subsequent allogeneic HSCT
Measured: 5 years
Stratum 1:Event free survival (EFS)
EFS assessed between treatment start until the date of the earliest of these events: death, progression or off protocol-treatment for any reason using the Kaplan-Meier method
Measured: Day 1 (treatment start) to 5 years
Stratum 1: Overall Survival (OS)
OS assessed between treatment start until death due to any cause using the Kaplan-Meier method
Measured: Day 1 (treatment start) to 5 years
Stratum 2: Overall response
Morphological overall response, defined as either CR or CR as complete remission (CR), CR with incomplete hematologic recovery, CR with incomplete count recovery or MLFS. For patients with MDS/CMML, overall response, defined as either CR or modified CR mCR with haematological improvement (HI) at the end of cycle 1
Measured: 4 weeks
Stratum 2: Minimal Residual Disease (MRD) response
Response is defined as MRD negativity with and without morphological complete remission (CR), at low level molecular MRD with CR and MRD relapse (coversion MRD negativity to positivity) at the completion of cycle 4.
Measured: 16 weeks
Stratum 2: Radiologic response
Response evaluation by 18F-FDG-PET/CT, based on the 5-point scale Deauville criteria for complete metabolic response (defined as as Deauville Score (DS) 1, 2, or 3) or for partial metabolic response (defined as DS of 4 or 5 with decrease in number or activity in bone marrow/EMD disease) at the the completion of cycles 4, 6, 9 and 12
Measured: 16, 36 and 48 weeks
Stratum 2: Dermal clinical response
Dermal clinical improvement based on the static investigator global assessment (IGA) 5-point disease severity scores, where higher score indicate more disease, defined as as disease severity score of 1 (almost clear) or 0 (clear) and at least a two grade/point decrease in severity score relative to baseline the completion of cycles 4, 6, 9 and 12
Measured: 4, 24, 36 and 48 weeks
Stratum 2: Dermal therapeutic response
Dermal therapeutic improvement based on the static investigator global assessment (IGA) 5-point disease severity scores, where higher score indicate more disease, defined as decrease of at least two points relative to baseline the completion of cycles 4, 6, 9 and 12.
Measured: 4, 24, 36 and 48 weeks
Stratum 2: Event free survival (EFS)
EFS assessed between treatment start until the date of the earliest of these events: death, progression or off protocol-treatment for any reason assessed
Measured: Day 1 (treatment start) up to 5 years
Stratum 2: Overall survival (OS)
OS assessed between treatment start until death due to any cause using the Kaplan-Meier method
Measured: Day 1 (treatment start) to 5 years
Timeline
From the start of the study to its completion; the mark is today. Estimated dates are the sponsor’s plan.
- First posted13 Jul 2022
- Study start29 Jul 2022
- Primary completion31 Aug 2023
- Study completion31 Aug 2023
Why it stopped: commercial reason
Resources
- Official record on ClinicalTrials.govThe registry entry this page is built from, with its full change history.
- Other trials for Acute Myeloid LeukemiaStudies of the same condition, open and under way.
- What the trial phases meanHow a treatment moves from first tests in people to approval.
More details
For doctors and researchers: how the study is designed, who runs it, and its registry IDs.
Study design
- Study type
- Interventional
- Phase
- Phase 1
- Primary purpose
- Treatment
- Allocation
- Non-randomised
- Intervention model
- Sequential
- Masking
- None (open label)
- Enrolment
- 0 participants (actual)
Sponsor and investigators
- Lead sponsor
- Racura Oncology Ltd
- Sponsor type
- Industry (pharma, biotech, devices)
- Collaborators
- Astex Pharmaceuticals, Inc.
- Responsible party
- Sponsor
- Investigators
- Marinella Messina, PhD, Study director, Clinical Director
IDs, dates and publications
- ClinicalTrials.gov ID
- NCT05456269
- Sponsor's protocol ID
- RAC-006
- Acronym
- BISECT
- Status last verified
- Sep 2023
- First submitted
- 4 Jul 2022
- Last updated
- 3 Oct 2023
- Results posted
- No
- Data monitoring committee
- Yes
- FDA-regulated drug
- No
- FDA-regulated device
- No
- Individual data sharing
- No